ClearanceBrief
Recall Z-2012-2017 ยท BWN Table And Attachments, Operating-Room

The Anspach Effort, Inc.

8.0cm Medium Attachment Product Usage: Pneumatic system

DateOct 6, 2016
StatusTerminated
ReasonSupplied Directions for Use (DFU) did not contain a recommended service interval.
Root causeUnder Investigation by firm
ActionConsignees were sent a recall notice via mail, dated 10/10/2016. In the notice, the firm notifies consignees of the Directions For Use (DFU) correction that will include recommended servicing intervals. All DFUs distributed after 09/28/2016 will have the correct DFU. The recalling firm instructs consignees to review the service intervals provided for product received, forward the notification to necessary parties and/or facilities, and complete the attached Verification Form. Complete Verification Forms are to be sent by fax to 877-546-5069 or by email to Anspach4870@stericycle.com. Consignees
Quantity1802
DistributionWorldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K011444ANSPACH EMAX DRILL SYSTEM
The Anspach Effort, Inc., Aug 8, 2001